| Literature DB >> 28371487 |
Bhumika Chaudhary1, Ashish Kulkarni1, Ajay Kumar Jena1, Masashi Ikegami1, Yosuke Udagawa2, Hideyuki Kunugita2, Kazuhiro Ema2, Tsutomu Miyasaka1.
Abstract
It is well known that the surface trap states and electronic disorders in the solution-processed CH3 NH3 PbI3 perovskite film affect the solar cell performance significantly and moisture sensitivity of photoactive perovskite material limits its practical applications. Herein, we show the surface modification of a perovskite film with a solution-processable hydrophobic polymer (poly(4-vinylpyridine), PVP), which passivates the undercoordinated lead (Pb) atoms (on the surface of perovskite) by its pyridine Lewis base side chains and thereby eliminates surface-trap states and non-radiative recombination. Moreover, it acts as an electron barrier between the perovskite and hole-transport layer (HTL) to reduce interfacial charge recombination, which led to improvement in open-circuit voltage (Voc ) by 120 to 160 mV whereas the standard cell fabricated in same conditions showed Voc as low as 0.9 V owing to dominating interfacial recombination processes. Consequently, the power conversion efficiency (PCE) increased by 3 to 5 % in the polymer-modified devices (PCE=15 %) with Voc more than 1.05 V and hysteresis-less J-V curves. Advantageously, hydrophobicity of the polymer chain was found to protect the perovskite surface from moisture and improved stability of the non-encapsulated cells, which retained their device performance up to 30 days of exposure to open atmosphere (50 % humidity).Entities:
Keywords: hole-transport layer; lead halides; lewis base; perovskite solar cells; poly(4-vinylpyridine)
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Year: 2017 PMID: 28371487 DOI: 10.1002/cssc.201700271
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928